2012
DOI: 10.1111/j.1440-1754.2012.02451.x
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A clinical audit of antithrombin concentrate use in a tertiary paediatric centre

Abstract: This data provides the basis for future investigations of the specific biochemical changes accompanying ATC administration and the development of paediatric-specific evidence-based guidelines for ATC use.

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Cited by 13 publications
(15 citation statements)
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References 18 publications
(24 reference statements)
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“…Mean UFH doses to achieve a target anti-factor Xa activity pre-and post-ATC administration were 28 (95% CI, 24-32) and 19 U/kg/hr (95% CI, [16][17][18][19][20][21][22], respectively, for children 12 months old or younger (p < 0.0001) and 25 (95% CI, [19][20][21][22][23][24][25][26][27][28][29][30] and 19 U/kg/hr (95% CI, [11][12][13][14][15][16][17][18][19], respectively, for children older than 12 months (p < 0.001). The anti-factor Xa activity preand post-ATC administration was 0.21 (95% CI, 0.17-0.25) and 0.47 U/mL (95% CI, 0.37-0.57), respectively, for children 12 months old or younger (p < 0.0001) and 0.24 (95% CI, 0.13-0.35) and 0.31 U/mL (95% CI, 0.23-0.39), respectively, for children older than 12 months (p = 0.07) ( Table 2).…”
Section: Resultsmentioning
confidence: 99%
“…Mean UFH doses to achieve a target anti-factor Xa activity pre-and post-ATC administration were 28 (95% CI, 24-32) and 19 U/kg/hr (95% CI, [16][17][18][19][20][21][22], respectively, for children 12 months old or younger (p < 0.0001) and 25 (95% CI, [19][20][21][22][23][24][25][26][27][28][29][30] and 19 U/kg/hr (95% CI, [11][12][13][14][15][16][17][18][19], respectively, for children older than 12 months (p < 0.001). The anti-factor Xa activity preand post-ATC administration was 0.21 (95% CI, 0.17-0.25) and 0.47 U/mL (95% CI, 0.37-0.57), respectively, for children 12 months old or younger (p < 0.0001) and 0.24 (95% CI, 0.13-0.35) and 0.31 U/mL (95% CI, 0.23-0.39), respectively, for children older than 12 months (p = 0.07) ( Table 2).…”
Section: Resultsmentioning
confidence: 99%
“…5 Exogenous AT III is often administered to patients with AT III deficiency who are receiving heparin infusions in an effort to increase efficacy of heparin, thus lowering the heparin infusion rates required to achieve therapeutic partial thromboplastin time or activated clotting time. 3,8 Additionally, higher AT III levels can result in more effective low-molecular-weight heparin doses. 10 The formulary AT III product at this institution is Thrombate III (Grifols, Research Triangle Park, NC).…”
Section: Introductionmentioning
confidence: 99%
“…The result is potential for a large amount of waste. 3 Safely rounding doses in young patients to available vial sizes may lead to cost savings.…”
Section: Introductionmentioning
confidence: 99%
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